HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934313Generated: October 31, 2026
Tert-Butyl nitrite → HCID 22466148, compound
https://huagongshe.com/reaction/1934313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 11131164 | HCID 11131164 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 22466148 | HCID 22466148 | 90% |
Reaction Steps
With ice-cooling, initially 9.5 g (92 mmol) of tert-butyl nitrite were added dropwise to a solution of 20 g (62 mmol) of 2-chloro-5-(3-chloro-5-trifluoromethyl-2-pyridyl)-4-fluoroaniline in 40 ml of trifluoroacetic acid, and—with strong evolution of gas—6 g (92 mmol) of sodium azide were then added a little at a time. The mixture was stirred for 16 hours, and a further 15 ml of trifluoroacetic acid and 1.7 g (17 mmol) of tert-butyl nitrite were then added to the reaction mixture. Stirring was subsequently continued for another 30 minutes, and the mixture was then poured onto 0.3 l of ice-water. The resulting solid fraction was separated off and washed with 50 ml of water. For purification, the crude product was initially dissolved in 100 ml of toluene. The resulting toluene phase was then washed with saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate and finally concentrated. Yield: 90%;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06383986B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-67f327fee3944433af4682903b7060c1 |
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| Source note | uspto-grants-2002_05 |
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